Canonical Allele Identifier: CA633644799

Gene: RRAS

Linked Data

• dbSNP Id: rs1224001494
• gnomAD v2: 19-50139631-C-CG
• gnomAD v3: 19-49636374-C-CG
• gnomAD v4: 19-49636374-C-CG
• MyVariant Identifiers: chr19:g.50139631_50139632insG (hg19) ; chr19:g.49636374_49636375insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636380dup , CM000681.2:g.49636380dup	GRCh38
NC_000019.9:g.50139637dup , CM000681.1:g.50139637dup	GRCh37
NC_000019.8:g.54831449dup	NCBI36
NG_042222.1:g.8769dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+244dup MANE Select	ENSP00000246792.2:n.453+244dup
ENST00000246792.3:c.453+244dup	ENSP00000246792.2:n.453+244dup
ENST00000601532.1:n.593+244dup
NM_006270.3:c.453+244dup	NP_006261.1:n.453+244dup
NM_006270.4:c.453+244dup	NP_006261.1:n.453+244dup
NM_006270.5:c.453+244dup MANE Select	NP_006261.1:n.453+244dup